Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP767723.RAVIGXpvgXYN2YLSnNsPa6doj2Cewk0tUIHf3Fl3Zve60130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP767723.RAVIGXpvgXYN2YLSnNsPa6doj2Cewk0tUIHf3Fl3Zve60130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP767723.RAVIGXpvgXYN2YLSnNsPa6doj2Cewk0tUIHf3Fl3Zve60130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP767723.RAVIGXpvgXYN2YLSnNsPa6doj2Cewk0tUIHf3Fl3Zve60130_provenance.
- befree-2016 importedOn "2016-02-19" NP767723.RAVIGXpvgXYN2YLSnNsPa6doj2Cewk0tUIHf3Fl3Zve60130_provenance.
- NP767723.RAVIGXpvgXYN2YLSnNsPa6doj2Cewk0tUIHf3Fl3Zve60130_assertion wasGeneratedBy ECO_0000203 NP767723.RAVIGXpvgXYN2YLSnNsPa6doj2Cewk0tUIHf3Fl3Zve60130_provenance.
- NP767723.RAVIGXpvgXYN2YLSnNsPa6doj2Cewk0tUIHf3Fl3Zve60130_assertion wasDerivedFrom befree-2016 NP767723.RAVIGXpvgXYN2YLSnNsPa6doj2Cewk0tUIHf3Fl3Zve60130_provenance.
- NP767723.RAVIGXpvgXYN2YLSnNsPa6doj2Cewk0tUIHf3Fl3Zve60130_assertion SIO_000772 19808697 NP767723.RAVIGXpvgXYN2YLSnNsPa6doj2Cewk0tUIHf3Fl3Zve60130_provenance.
- NP767723.RAVIGXpvgXYN2YLSnNsPa6doj2Cewk0tUIHf3Fl3Zve60130_assertion evidence source_evidence_literature NP767723.RAVIGXpvgXYN2YLSnNsPa6doj2Cewk0tUIHf3Fl3Zve60130_provenance.
- NP767723.RAVIGXpvgXYN2YLSnNsPa6doj2Cewk0tUIHf3Fl3Zve60130_assertion description "[Somatic mutation of the AML1/RUNX1(RUNX1) gene is seen in acute myeloid leukemia (AML) M0 subtype and in AML transformed from myelodysplastic syndrome, but the impact of this gene mutation on survival in AML patients remains unclear.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP767723.RAVIGXpvgXYN2YLSnNsPa6doj2Cewk0tUIHf3Fl3Zve60130_provenance.